4.6 Article

Andrographolide and Its 14-Aryloxy Analogues Inhibit Zika and Dengue Virus Infection

Journal

MOLECULES
Volume 25, Issue 21, Pages -

Publisher

MDPI
DOI: 10.3390/molecules25215037

Keywords

Zika virus; dengue virus; andrographolide; HSPA1A; PGK1

Funding

  1. Newton Fund [FDA-CO-2561-6820-TH]
  2. Thailand Research Fund [BRG6080006]
  3. National Research Council of Thailand
  4. Mahidol University [NRCT5-RSA63015-03]
  5. Thailand Graduate Institute of Science and Technology (TGIST)

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Andrographolide is a labdene diterpenoid with potential applications against a number of viruses, including the mosquito-transmitted dengue virus (DENV). In this study, we evaluated the anti-viral activity of three 14-aryloxy analogues (ZAD-1 to ZAD-3) of andrographolide against Zika virus (ZIKV) and DENV. Interestingly, one analogue, ZAD-1, showed better activity against both ZIKV and DENV than the parental andrographolide. A two-dimension (2D) proteomic analysis of human A549 cells treated with ZAD-1 compared to cells treated with andrographolide identified four differentially expressed proteins (heat shock 70 kDa protein 1 (HSPA1A), phosphoglycerate kinase 1 (PGK1), transketolase (TKT) and GTP-binding nuclear protein Ran (Ran)). Western blot analysis confirmed that ZAD-1 treatment downregulated expression of HSPA1A and upregulated expression of PGK1 as compared to andrographolide treatment. These results suggest that 14-aryloxy analogues of andrographolide have the potential for further development as anti-DENV and anti-ZIKV agents.

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